Tuesday 3rd February 2015

(9 years, 9 months ago)

Grand Committee
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Motion to Consider
15:30
Moved by
Earl Howe Portrait Earl Howe
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That the Grand Committee do consider the Care and Support (Business Failure) Regulations 2014.

Relevant document: 17th Report from the Joint Committee on Statutory Instruments

Earl Howe Portrait The Parliamentary Under-Secretary of State, Department of Health (Earl Howe) (Con)
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My Lords, I come before the Committee today to introduce the draft affirmative regulations under Part 1 of the Care Act 2014. The regulations before us relate to some of the most important elements of the Care Act, which consolidated 60 years of fragmented legislation into a single modern statute built around the needs and outcomes of a person.

Following Royal Assent for the Care Act in May 2014, the Government published final statutory guidance and laid those regulations subject to the negative procedure before Parliament in October and November, as well as laying these regulations in draft. In keeping with the collaborative approach that we have sought to maintain through the development of these reforms, over the summer the Government conducted an extensive public consultation on the guidance and regulations, including draft versions of the regulations that we will consider today.

The consultation engaged the full spectrum of stakeholders including: people receiving care and support and their carers; social workers and other front-line practitioners; local authority commissioners; social care providers; national representative groups; and NHS bodies. In total, the consultation drew more than 4,000 responses from many different sources. Responses were carefully analysed and, where appropriate, changes were made to regulations.

I will briefly introduce each of the four statutory instruments. I turn first to the Care and Support (Business Failure) Regulations 2014 and the Care and Support (Market Oversight Criteria) Regulations 2014. I will address these together as they form the two pillars of our broader strategy to protect people from provider failure. There is a diverse provider market in adult social care where entry and exit is a regular occurrence. Local authorities are currently able to intervene to meet needs in relatively rare cases where services are closed at short notice and individuals are put at risk—and historically they have done so effectively.

The Care Act places specific duties on local authorities in Wales and England, and their broad equivalents in Northern Ireland, to temporarily step in and meet needs where a provider is no longer able to carry on because of business failure. The business failure regulations set out the meaning of “business failure” generally by reference to different types of insolvency, for example administration and winding up. This approach ensures that people receiving services are protected in the event that their provider enters insolvency, without diluting the core responsibility of providers to deliver care services under normal circumstances.

The social care market includes large care providers, operating across much of England, whose financial failure, were it to happen, would cause local authorities considerable difficulty in carrying out their business failure duties without early warning. One such recent example was in 2011 when Southern Cross, then the largest provider of residential services in England, was threatened with insolvency. Local authorities had no prior warning of its financial position. While few people eventually had to change care home, the Government recognised that the degree of worry for people receiving care and their families was unacceptable.

The Care Act accordingly places new duties on the Care Quality Commission to assess the financial sustainability of certain registered care providers. The CQC will do this by collecting and analysing financial information. The CQC may respond to significant risks identified to the financial sustainability of a provider by requiring it to develop a plan to mitigate any risks identified, or ordering an independent review of the business. Should the CQC be satisfied that a provider is likely to fail, it will provide relevant local authorities with an early warning and the information that they need to prepare adequately to protect the continuity of care for individuals. Where the CQC is not satisfied that the provider is taking all the necessary steps to return to financial health, or it feels that it has not been given the necessary information to assess financial sustainability, it is able to take a range of regulatory actions, up to and including the deregistration of the provider in question.

The Care and Support (Market Oversight Criteria) Regulations set the entry criteria for the CQC’s financial oversight regime. Any provider meeting those criteria will be subject to the CQC’s regulatory activities that I have described. They have been designed to capture those providers that—because they are particularly large, geographically concentrated or operate in a large number of local authority areas—would be “difficult to replace” were they to fail financially. It is important to note that inclusion in the regime is a comment not on the likelihood of failure but rather on the risks that would be posed should the provider get into difficulties.

The Care and Support (Children’s Carers) Regulations 2014 relate to the power in the Act for local authorities to support carers of children in a similar way to that in which they support carers of adults, setting out how the rest of Part 1 of the Act applies in this situation. It is important to note that this power applies only in the limited circumstances where carers of children have received a transition assessment in preparation for beginning to receive support under the adult statute, but the transition has not yet actually taken place.

The broad principle at work will be that adult carers of children are supported under children’s legislation, while adults caring for adults will be supported under the Care Act. This instrument is merely an acknowledgement that some flexibility in this regard may be desirable around the time of transition. The instrument has been carefully drafted to ensure that it does not replicate the support for carers of children under other legislation, so ensuring that there remains a clear division of responsibility. These regulations allow for flexible and personalised approaches to support, without forcing local authorities into unnecessary changes to different, broader policies for carers of children and of adults, which exist for good reasons.

Lastly, the Care and Support (Eligibility Criteria) Regulations 2014 set out the national eligibility criteria for adult care and support and carer support. All local authorities will at a minimum have to meet this threshold and cannot tighten their criteria beyond it, although they will have a power to meet needs that were not considered eligible. The national eligibility threshold has been set at a level where the person’s care and support needs, and their inability to achieve certain outcomes as a result, have or are likely to have a “significant impact on their well-being”. This is intended to have a similar effect to the eligibility level that the vast majority of local authorities operate at present. Together with funding announced in the 2013 spending round, this will allow local authorities to maintain the level of access to care and support when the new system is introduced in April 2015.

Given the critical importance of the eligibility criteria, the Government have been especially careful to ensure that they have taken account of the full views of all relevant stakeholders. The Department of Health carried out an extensive engagement to gather views on an initial version of the regulations from June to December 2013, and engaged the Personal Social Services Research Unit at the London School of Economics to evaluate the draft regulations against current practice. These findings informed the second version of the eligibility regulations that were consulted upon in summer 2014.

Alongside the consultation, the department asked PSSRU to evaluate the second draft of the regulations, working with 27 local authorities to compare the draft regulations with recent cases. We made a number of changes to refine the criteria on the basis of feedback and independent research. We have also worked closely with stakeholders to test the approach. I am confident that the final version before us fulfils the Government’s commitment to replicate the current access to care and support in setting the national criteria.

These regulations are required to meet fully some of the central aims of the Care Act: protecting people from the reality of provider failure and the extreme worry caused by its spectre; providing flexible and appropriate support for carers; and ensuring more consistency in people’s rights to care and support. I commend these statutory instruments to the Committee.

Baroness Wheeler Portrait Baroness Wheeler (Lab)
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I thank the Minister for his comprehensive introduction to these four important affirmative regulations. As he knows, I also have a take note Motion tabled for next week on the negative regulations on implementing the Care Act. Inevitably, there will be overlaps between today’s debate and next week’s but I hope that we can clear off some of the major issues today. The four SIs cover a number of important issues so, while we were happy to have them taken together to expedite the business of the Committee, I hope that the Committee will bear with me since there are a number of areas to cover in relation to implementation of the Care Act and the individual SIs. I also thank the Minister for the very helpful briefing meetings that he has had with Opposition Front Bench health team members on the regulations. He will know that both the Opposition’s health and local government teams are keeping a close watch on how the Care Act is being implemented, so we were grateful for the time that he took on this.

We believe strongly that this first phase of implementation has to be viewed across both the local government and health departments, and considered in the context of the huge funding pressures on local authorities, with a 40% cut in their funding since this Government took office. The Minister, of course, disputes this figure and others from independent bodies on the scale of local government cuts cross the piece and their devastating knock-on impact on social care. Whether the figures are from the King’s Fund, the Nuffield Trust or Age UK, they all put the scale of cuts to social care budgets in terms of billions of pounds.

Recent figures from the Association of Directors of Adult Social Services, with which the Department of Health has worked closely on the Care Act’s implementation, point to this year being the third year of continuing cash reductions and the fifth of real-terms reductions in spending on social care. It points out that, since 2010, social care spending has fallen by 12% while the number of those looking for support has increased by 14%. Social services departments have been forced to make savings of 26% in their budgets—the equivalent of £3.53 billion over the last four years. Compared to 2009-10, almost 300,000 fewer people over the age of 65 are receiving state-funded care.

On many previous occasions, the Minister has set out the additional funding being made available for Care Act implementation—and, despite the challenges, the recent DH stock-take shows encouraging overall progress in local authorities’ readiness for the phase 1 implementation from April 2015. Like the department, we commend the role of the joint LGA/ADASS/Department of Health programme management office. We fully recognise the scale and extent of the work that has gone into consultation exercises with stakeholders, the drafting of the regulations and guidance and the joint working on implementation with local authorities.

However, the same stock-take also makes clear councils’ continuing concerns about the adequacy of funding in the face of modelling which shows increasing support needs for local authorities around IT, workforce, information advice, carers and market shaping. Workforce capacity is a particular concern. The LGA view is that these aspects of implementation of the 2015-16 reforms may be underfunded by as much as £50 million.

Before moving on to the regulations, perhaps I may refer quickly to the Government’s plans to close down the Independent Living Fund in June 2015. We seek reassurances from the Minister that the funds transferred to local authorities from that fund will continue to be used to provide vital support for the disabled people who currently depend on it to be able to live independently in the community and have the same rights, choices and chances as any other citizen. My understanding is that it will be for individual authorities to make decisions on how the resources from the fund will be applied. Will the Government issue guidance to help protect the thousands of disabled people currently receiving ILF support who are affected by this decision? How will they ensure that the money is not just diverted into helping to fund the Care Act implementation or into general funding support for social care services?

The care and support regulations on the market oversight criteria, the interlinking negative regulation on market oversight information—covered by my take note Motion next week—and the business failure regulations are about trying to prevent the sort of problems witnessed in 2011 with the collapse of Southern Cross Healthcare, as set out by the Minister, by empowering the Care Quality Commission to monitor and obtain financial information from providers to check their financial stability and spot the early warning signs of potential difficulties and failure. The aim is to protect vulnerable people and their families if there is provider failure, to ensure that local councils have both early warning and support to be able to maintain vital continuity of support and to ensure that no one depending on the service will suffer.

15:45
We all agree that, to do that, the CQC has to have the right powers, resources and expertise to scrutinise the very complicated company financial structures and accounts of care providers, which are often multi-company set-ups both here and abroad, making financial assessment and monitoring a huge and complex task. My honourable friend Liz Kendall questioned the Health Minister, Norman Lamb, closely on this when the regulations were dealt with in the Commons. The Minister expressed his full confidence in the CQC powers across the range of the provisions in the Act and the regulations, including, as the Minister pointed out, assessing finances, requiring organisations to take steps to return to financial health if there are problems, requiring the provider to undertake an independent review and producing a plan to mitigate financial risk.
Those are complex expert tasks indeed, and in the light of that I am sure that the Government now regret saying in the consultation that they expected CQC information-gathering to be “light touch”. I ask the Minister to reassure the Committee that he recognises the scale and extent of the task facing the CQC, involving detailed monitoring, scrutiny and assessment under the criteria set out in the regulations, equating to 400 registered providers across about 4,000 locations. Will he commit to ensuring that the CQC is effectively resourced to undertake this work?
Under the Care Act, local authorities are required to step in and provide care where a provider is no longer able to carry on because of business failure. I also ask the Minister what guidance, support and funding will be given to local authorities to help them cope with ensuring that there is continuity of care and that they are given the concrete practical advice they need. There is concern that the current focus is on the duties faced by local authorities rather than on the vital support to be provided when a major failure occurs.
Finally on these regulations, I note that the Joint Committee on Statutory Instruments has drawn the attention of the House to the market oversight information regulations being “defectively drafted”. I assume that we will be covering this next week but I ask the Minister to provide for noble Lords—prior to the debate, if possible—information on the department’s response to the Joint Committee’s comments and notice of any proposed changes that need to be made as a result of the committee’s findings on this and the two other SIs to which the committee refers.
Next, I turn to the children’s carers regulations. We now hear that we have an important interface between the Care Act and the Children and Families Act concerning the extent to which the arrangements for the carers of disabled children fall under either Act. Many hours and days were spent during the passage of both pieces of legislation on trying to address the concerns of parent carers. The provisions in these regulations deal with the preparation of carers of disabled children for the child’s transition to adult care and support. I understand that there has been considerable discussion with carers’ organisations over these transitional arrangements and that progress has been made, but there is still strong concern that carers in this situation have weaker rights than carers caring for adults.
As I understand it, under these regulations someone caring for a child in transition who is eligible for support would be able to receive services for the child, such as replacement care, only if this were provided by children’s social services. However, under the children legislation, there are no nationally set eligibility criteria for carers, which means that the carer of a child in transition who needs support as a carer will not have as clear a right to this support as an adult caring for another adult covered by the Care Act. The important interlink here is the need for regulations or statutory guidance setting out the operation of the new duties to carry out parent carers’ assessments for local authorities. There is no sign of these coming, and only belatedly have draft regulations on assessments for young carers been issued for consultation. Can the Minister comment further and update the Committee on this? Does he acknowledge that, without these, local authorities will be left without clarity about implementing the new rights? What plans do the Government have to support local authorities in implementing the new rights for parents and young carers?
There is also strong concern about the rights of carers of disabled children under the age of 16 who do not have legal parental responsibilities, such as siblings, grandparents and other family members or friends who are not covered by either the care or the families legislation. Can the Minister confirm that the relevant parts of the Carers (Recognition and Services) Act 1995 will be retained to ensure that such carers do not lose any existing rights to a carer’s assessment?
My final issue on the subject of parent carers concerns those caring for a disabled child as well as an adult with care needs. It is more an issue of practice rather than official guidance. It would be complex for those working with carers to bring together the legal duties and practice from the two pieces of legislation and it is important that practitioners are supported to develop best practice in this area. What are the Government doing to support the workforce to understand how to knit together the two pieces of legislation in more complex family situations such as these?
The final regulations we are discussing today concern the key issue of eligibility criteria for care and support. We cannot consider these without first acknowledging the deep concerns of the organisations that work with older and disabled people that the objectives of the Care Act of early intervention, prevention and promotion of well-being cannot be achieved with the eligibility criteria set at the level in the regulations. The Care and Support Alliance, which represents 75 leading charities, estimates that this will leave 340,000 older and disabled people without the support they need to do things as basic as get up, wash, dress and eat.
The alliance rightly argues that if older people do not get the care and support they need it would be bad for them as well as costing the taxpayer more because their health will suffer and they will need to go into more expensive hospital or residential care. The strong fear is that the mix of the “unable to achieve two or more” of the activities in the list of the 10 outcomes, combined with the caveat that the local authority must deem such an inability as having “a significant impact” on the adult’s well-being, leaves open to interpretation by each local authority what constitutes a significant impact on well-being. Some of the language in these regulations is seen by many as vague and open to misinterpretation.
We support national eligibility criteria which limit postcode lotteries and variations across the country and we do not consider that the current regulations achieve this. How does the Minister consider that the postcode lottery situation will be avoided? The original draft regulations referred to one or more specified outcomes and it would be helpful to hear why the criteria were tightened up following the consultation.
We know that with the current financial pressures councils are deeply concerned about the potential costs of the new eligibility criteria. Their fear, in contrast to the stakeholder concerns, is that the new definition of “substantial” and the wider well-being perspective may in practice turn out to be more generous than the current definition, despite the firm view at the Department of Health that the regulations have been drawn in such a way as to be very similar if not the same. The LGA is calling for financial compensation for councils which are shown, under the monitoring framework being developed by ADASS, to have incurred extra costs over and above their 2015-16 allocation. Can the Minister reassure councils that this will be the case? Does he agree with the LGA view that the reality is that the eligibility will continue to be a very subjective process under each council?
On a wider issue, the Secondary Legislation Scrutiny Committee—we have copies of its report here today—has rightly pointed out the huge communications and information challenges ahead for the Government and local authorities in explaining the new system and how it operates to applicants. As it said, the extensive guidance that has been drawn up at 500 pages,
“is going to be beyond the understanding of most applicants”—
an understatement if there ever was one. Can the Minister tell the Committee what strategies and work are in place to address this situation? Will he undertake to have further discussions with stakeholders on this key issue and work closely with them to ensure effective information, communications and support for the applicants, their carers and families as they try to tackle the mound of form-filling and paperwork that is potentially involved?
Finally, on pension pots, is the Minister in a position to update the Committee on any progress that has been made concerning the question of assessments for income-related benefits and the implications for care and support under the Care Act arising from the pensions flexibility provision in the Pension Schemes Bill? My noble friend Lord Hunt raised this matter during the debate on the deferred payments regulations before Christmas, but the subsequent response of the noble Baroness, Lady Jolly, in January did not answer the key question of what happens in the light of the effective breaking down of the distinction between a savings account and a pension under the pensions flexibility arrangement.
During the Pension Schemes Bill debate on this issue there was little evidence of joined-up working and discussion between the DWP and the Treasury, let alone of discussions with the Department of Health on the implications for the pension pots of applicants applying for support under the Care Act. Can the Minister confirm that the DoH is involved in discussions on this and that the Government will respond on this issue to deal with the situation under the Care Act before the Third Reading of the Pension Schemes Bill, which is tomorrow?
Lord Lipsey Portrait Lord Lipsey (Lab)
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My Lords, it is a great pleasure to follow my noble friend Lady Wheeler, who has achieved the rare feat of matching the Minister in both her knowledge of the subject and the eloquence with which she expressed it. I shall raise one or two points on just two of today’s regulations. The first is the market oversight criteria regulations—which, in principle, I strongly support. A few alarm bells began to ring in my skull when I saw that the body to be responsible for this is the CQC. My mind drifted back nearly a decade, I suppose, when we were in this Room debating the amalgamation of three regulators, proposed by the then Government, into the CQC. I remember speaking with all the eloquence that I could muster to explain why this was going to be disastrous, and the noble Lord, Lord Darzi, the then Minister, explaining with great eloquence why I was completely wrong. After that, the noble Lord and I would go outside and he would say, “I totally agree with you, David; this is an act of absolute madness”. I am afraid that for years so it proved.

I regard the CQC as on probation. It has new management. David Behan, the chief executive, is a man for whom all of us, I think, have the greatest respect. There are examples in which the CQC is improving its practice but it is still only on probation, which in itself does not provide me with the complete reassurance that I should like. More seriously, it is all very well having market oversight, but you need the resources to do it. I have done a little back-of-the-envelope calculation based on the Explanatory Memorandum, which suggests that the CQC will spend £6,000 per chain monitoring whether it is in financial trouble. Frankly, £6,000 does not buy much of a top accountant’s time. So while I should like to think that the CQC will pick up readily in advance of crises that there are problems, I doubt whether it is resourced to do so. The Minister and the Government should satisfy themselves that this job will be done and is not just a paper exercise so that, if something goes wrong, they can say that they did something about it. In practice, that will not be effective.

It is not entirely accurate to say that the eligibility criteria regulations translate into legislation the present criterion of substantial. Indeed, it has been argued that this is a slightly more liberal definition than the present substantial definition of what creates eligibility. But it is also not wholly inaccurate. I do not have any objection to this. I have read the useful briefing provided by the Care and Support Alliance but I am not convinced that, given the shortage of finance, to which I shall return in a moment, it would make sense to impose a much looser definition of eligibility and substantial, as recommended by Dilnot—particularly in view of the financial situation in social services.

I know that figures get bandied about for ever on this. I chose to take one from the Department of Health’s publication of March 2014 in which it said that spending on adult social services had fallen by 8% in the previous two years. Since the Government say that that is true, it must be true. Incidentally, we are seeing a folly in public finance which deserves to be highlighted. When you ring-fence one bit of public finance or guarantee it in real terms, that leads to more pressure on other forms of public finance. Because healthcare is ring-fenced and maintained in real terms—I am not arguing about whether the numbers are right—social services ends up taking more of the brunt.

15:59
I know that ingenious methods have been used by the Government to try to transfer money from one to the other without being caught doing so in terms of a breach of their health commitments, but it makes it all more complicated. Whatever approach you take to the necessary closer integration of health and social care, one budget has always seemed to me to be the absolute secret of it—and nothing here moves us greatly towards that.
My second concern is that it appears that one is setting here—indeed, I think the Minister almost said as much—some sort of national standard where, wherever you live in the country, you are bound to get a certain amount of help if you have these substantial care needs. However, I refer back to a report of the Audit Commission. I am afraid I do not have it to hand; it is a number of years old, but it was very striking at the time. Whether you get help from your local council depends not so much on which council you live under, but on who the council happens to send round to see you. To caricature it: if you get a social worker who was brought up, as my wife was in the good old days, when social workers were advocates for their clients, and their job was to argue for the most money possible for them, you may get help despite having only relatively minor impairments; if you get one of the modern breed who has been told that their career prospects depend entirely on denying as many people as possible the help they need, you might get another verdict. This gives the illusion that it is removing national disparities across the nation. It is removing the geographic postcode lottery, but it is not removing the social-worker-you-get lottery—and that, according to the Audit Commission, is a more serious lottery.
Also, these verdicts will be even more significant in future than they are at present. At the moment, yes, the assessment determines whether you get local authority-supported help with your needs—whether you have to contribute towards the cost of that through the means test or whether you get it free is a separate issue—but, under the new regime, it will determine another thing, too: it will be what decides whether you start the meter ticking for eligibility towards the £72,000 Dilnot care-cost cap. Old people will have much more at stake in these assessments even than they do now. Their families will have a huge amount at stake, because if they are turned down and the meter does not start running, it will be longer before their care costs are paid for.
All this will come out in the wash, but it will be a very painful wash. There will be an awful lot of appealing going on; an awful lot of people who feel very ill treated because they do not get rated as having substantial needs, when they feel that their needs are substantial; a great many cross relatives; a great many older people feeling unfairly treated. Of course, there will be mistakes and anomalies and problems.
We all know the problems that arise with an old person when a social worker comes round. The person can hardly drag themselves out of bed and toilet themselves or whatever, but when the social worker comes, they think, “Christ, if I’m not careful, I might get taken into care”. So they say. “I am fine. I can bounce about my flat under my own steam with no difficulty at all”. Well, of course, the social worker then fills out the forms saying that no help is needed, whereupon the old person flops back into bed and stays there without the help they actually need for another year or two until someone tries again. I put it in simple and no doubt over-flamboyant language, but this is a reality that we need to face up to.
Although I have no substantial objection to these regulations, this is the beginning of the story, not the end of the story. There is a great deal to be worked through here and a great deal to be thought through by the Government, by local government and by the organisations that represent those in need of care. I am sure that it will need to be debated in the House—and further action taken as the months and the years go by.
Baroness Pitkeathley Portrait Baroness Pitkeathley (Lab)
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My Lords, I will speak briefly on two of these regulations: those relating to the eligibility criteria, following on from my noble friend Lord Lipsey, and, first, the children’s carers regulations.

Some noble Lords in the Room will remember, when the Children and Families Bill went through this House, the struggle that we had to get parent carers recognised at all in the legislation. All credit to the Minister for finally recognising that parent carers had rights. However, there is now a serious problem because the regulations that we were promised would be issued along with the regulations under the Care Act have not in fact been issued. We have therefore left local authorities without clarity or direction about how to implement these new rights for parent carers—rights which we won with such difficulty but with eventual recognition from the Minister.

I ask the Minister, as did my noble friend, when the Government intend to publish statutory guidance on the new rights for parent carers under the Children and Families Act, why the statutory guidance was not issued at the same time as the guidance under the Care Act, and what plans they have to support local authorities in implementing the new rights for parent carers and young carers. I also support what my noble friend Lady Wheeler said about those carers who are left high and dry—the carers of disabled children who do not have parental responsibility. They are not covered by either piece of legislation and are left with a rump of rights under the long-outdated Carers (Recognition and Services) Act 1995. We really do need to clear that up.

I turn to the issue of eligibility criteria. As everybody knows, the Care Act creates an equivalent duty on local authorities to meet the care and support needs of adults and carers alike. In doing so, it puts carers of adults on the same legal footing as adults with care needs. This was a hugely significant legal development, giving carers the clearest rights ever to support in their caring role, and it is greatly welcomed. However, the Government’s decision to set the minimum threshold at the level at which local authorities are already providing support is a cause for huge concern. As we heard from my noble friend, the historic underfunding of social care has left thousands of older and disabled people without access to the care that they need, and has heaped pressure on to family carers, who are increasingly stepping in to provide care at great personal, societal and economic cost.

ADASS reports that spending on social care has been reduced by some 26% in the past four years. It is absolutely vital that a sustainable level of funding is put in place for social care, setting the funding mechanisms which will deliver the amount of money that we need to tackle the existing gap between need and supply and to keep pace with growing demand—and the demand is growing. The number of carers who care for 50 hours or more per week is rising faster than the number of the general carer population—Carers UK estimates that there has been an increase of 25% over the past 10 years. Despite the ongoing rise in the number of carers in the UK, the number receiving carers’ assessments and carer services from their local authorities is falling. I fear that that situation will only get worse. Carers are going without food and cutting back on essentials. Those who care for 35 hours or more a week are twice as likely to be in bad health as non-carers, with the knock-on effect that that will have on their own health in the future. Therefore, I believe that we have to look very carefully at the levels of funding and at what the eligibility criteria mean.

So far as carers are concerned, the Care Act is all that I could wish for—and have been working for for almost the last 30 years. It is ironic that it is being implemented at a time when budgets are so tight that the rights of carers may be threatened, not enhanced.

Earl Howe Portrait Earl Howe
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My Lords, I am grateful to all noble Lords who have spoken for their questions and comments on these regulations. I turn first to the regulations relating to business failure duties and market oversight criteria, and in particular to the question posed by the noble Lord, Lord Lipsey, about why we have chosen the CQC as the regulator in this regard. I say openly to him that it was a finely balanced decision. We were confident that we had a choice between the CQC and Monitor. Either could have performed the role. Last year, the Health Select Committee recommended that the Government should reconsider their decision to choose the CQC rather than Monitor to undertake this regulatory function.

However, as set out in the committee’s report, there is a close correlation between poor quality and poor financial performance. It recognised that for this reason the CQC is well placed to perform the function. The CQC is gearing up to do that. It recognises that it needs additional skills to assess the financial sustainability of providers. It does not yet have these core skills in-house. The CQC has procured external consultants to assist in designing its new regime and the resources needed to operate it, which will comprise a mix of internal and external expertise. That will ensure value for money. It is recruiting a number of highly experienced specialists in accounting and insolvency who will be responsible for undertaking the financial sustainability assessments of providers in the regime on an ongoing basis.

The department will support the CQC to carry out this function by providing additional funding. I hope that that provides the noble Lord with some confidence that the CQC is well capable of undertaking this task. The CQC has published draft proposals on how the market oversight regime should operate. A four-week public consultation began on 29 January. Revised final guidance will be published in early April.

As regards the process of gathering financial information, which was referred to by the noble Baroness, Lady Wheeler, the CQC has the power to require a provider to supply the information specified. The provider cannot refuse without risking enforcement action by CQC. The CQC’s aim is that the information it requests from providers will be the same as the provider’s own board would use to assess how the business is faring. It will be light touch in the sense of not onerous. The CQC has a duty to minimise burdens on businesses. However, its overriding duty is to protect vulnerable people by understanding providers’ finances and sustainability, and giving early warning of any likely failure to local authorities to help them intervene. It will require information in a proportionate way to deliver this duty.

The noble Baroness also referred to the need to support local authorities to carry out their temporary duties when a care provider fails. We recently published statutory guidance outlining local authorities’ roles and responsibilities in the event of business failure to support them in this area. In addition, the department plans to work with the Association of Directors of Adult Social Services to develop further guidance on contingency planning for provider failure, which should be available by the summer of 2015. The department has also commissioned guidance which will help local authorities to assess the financial sustainability of their local care market and individual providers within it that are not subject to the market oversight regime.

As regards the Care and Support (Children’s Carers) Regulations, concerns were raised by the noble Baronesses, Lady Wheeler and Lady Pitkeathley, around children’s carers, and in particular the new right to assessment for carers in the Children and Families Act which covers adults caring for disabled children only when they have parental responsibility. The Government will address this issue through the Care Act 2014 and the Children and Families Act 2014 (Consequential Amendments) Order 2015, which will be laid in draft before Parliament very shortly. The order will effectively save Section 1 of the Carers (Recognition of Services) Act 1995 in so far as it applies to adults caring for disabled children who do not have parental responsibility. This means that such adults will continue to have a specific right to ask for an assessment under the 1995 Act if they are caring for a child being assessed under the Children Act 1989 or the Chronically Sick and Disabled Persons Act 1970. I hope that that is helpful.

As to the specific right of adults caring for children to support to meet eligible needs, care and support for children and their carers takes place in a different context to that covered by the adult statute. Children’s legislation rightly gives primacy to the welfare of the child and this is reflected in the way the legislation works. With that said, of course the Government recognise the enormous contribution of carers of disabled children and the sacrifices they often make in taking on these caring roles. That is why the Children and Families Act includes a specific right to assessment for parent carers of such children and a requirement that in carrying out these assessments local authorities must now have regard to the well-being of a parent carer. This mirrors the definition of well-being in the Care Act, which is of course also the basis for considering the impact on well-being through the eligibility criteria.

16:15
I do not believe that the concern of the noble Baroness, Lady Wheeler, that carers of children will be left with inferior rights during transition, is well founded. The regulations stipulate that services may not be provided to a child to meet the needs of their carer under this legislation, but we are not at all saying that providing services to a child would never be an appropriate response to supporting their adult carer. The stipulation is simply about division of responsibility, specifically the principle that care and support for children should always be provided under children’s legislation. Where children under 18 are supported, this should always happen under children’s legislation—usually the Children Act 1989. This of course is also the rationale for a parent carer’s broader right to assessment being inserted into the Children Act 1989 rather than included in the Care Act. Transition is a time when it is particularly important to be clear about the division of responsibility, so it would not be appropriate to create an overlapping set of legal entitlements for carer support for children based on whether or not their adult carer has had a transition assessment.
I come lastly to the Care and Support (Eligibility Criteria) Regulations 2014. Perhaps I may, first, briefly cover the comments made by the noble Baroness, Lady Wheeler, about funding for adult social care in general. We know that there have been pressures on local authority budgets and it would be idle to pretend that local authorities have not felt that pressure very acutely across the board. Since 2010 we have allocated additional funding for the NHS each year to support social care. That funding is worth £1.1 billion in the current financial year. Social care expenditure has decreased in real terms but by a great deal less than local authority expenditure in other areas.
We can also look forward to next year when the better care fund will be established to provide better integrated care. One of its conditions is to improve the delivery of health and social care by preventing people reaching crisis point. The vast majority of the £5.3 billion that has currently been allocated to the fund is being spent on social care and out-of-hospital community health services.
The noble Baroness asked whether it followed that the 12% reduction in local authority budgets and the knock-on effect in care spend, plus the 14% growth in the numbers of elderly and vulnerable people, equates to a 26% shortfall. I cannot agree with her maths on that. The two figures are for different issues and are not comparable. For a start, not all of the additional elderly people will be eligible for care and support.
Lord Foulkes of Cumnock Portrait Lord Foulkes of Cumnock (Lab)
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My Lords, if the Minister is going to correct my noble friend, could he say what the combined effect will be in percentage terms?

Earl Howe Portrait Earl Howe
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I shall have to take advice before answering, but I will be happy to answer the question as soon as I receive inspiration.

Implementing the Care Act will be a challenge for local government, and takes place in the context of competing policy and financial pressures. However, we have already announced £470 million in total for the cost of the new duties in the Care Act which come into effect in April 2015. We have made substantial revisions to our impact assessment, following work with local authorities, to reflect changed assumptions on costs. This will mean acknowledging greater costs for carers in 2015-16 and beyond. We have recognised that.

In the first year, we will create a new carers grant to target this funding where it is most needed. As a result of this work, we believe that implementation of the Care Act will be affordable to local authorities in 2015-16. We will take further steps with the LGA and ADASS to agree a process for monitoring the costs in-year during 2015-16, to check on our assumptions and to provide evidence for the next spending review. Affordability is not just about the overall funding. We are also investing in a large suite of materials to help councils implement the Act effectively.

As regards the question posed by the noble Lord, Lord Foulkes, I am advised that the calculation that he seeks is not a simple one. I will need to write him a letter. I hope that he will allow me to do that. I shall try to be as explicit as I can in that letter.

Lord Foulkes of Cumnock Portrait Lord Foulkes of Cumnock
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It is certainly not a simple calculation, and I think my noble friend was near the mark. Would the Minister send a copy of the letter to all the Members present?

Earl Howe Portrait Earl Howe
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I will be very happy to do so.

The noble Baroness, Lady Wheeler, referred to the closure of the Independent Living Fund, and asked for the Government to provide guidance in the light of that. In response to the views of stakeholders during the consultation, we have provided guidance on how local authorities should manage the transition to social care for people previously receiving ILF funding. The guidance is included in the Care Act guidance that has now been published.

Both the noble Baroness, Lady Wheeler, and the noble Lord, Lord Lipsey, questioned the words “significant impact on well-being”. In particular, they expressed concern that there might be a variation of interpretation of that phrase. One of the core principles of the Care Act is that the person is central to the new care and support system, and that support is built around their needs and the outcomes they want to achieve. Considering the impact on the person’s well-being in deciding on their eligibility will make the determination personal to them. This recognises that people with similar needs and inabilities to achieve certain outcomes may have different eligibility determinations because the impact on their well-being is different.

It is important that there is consistency in approach in how the eligibility criteria are used. We have commissioned Skills for Care to develop training material and the Social Care Institute for Excellence to develop practice materials to support implementation of the eligibility criteria across authorities. Professional judgment will remain key to decision-making—this should not become a tick-box approach which does not focus on the person. We have never claimed that this will remove disparity. The system is person-focused, so it is inevitable and right that individual decisions will be made.

As regards the concern of the noble Baroness about requiring people to be unable to carry out two or more outcomes, and whether that would restrict access to care, this was an issue that was raised with the consultation version of the regulations, where there was concern that it would be impossible for people with mental health problems to become eligible due to how we described the outcomes that had to be considered. We addressed this in the regulations we are discussing today by converting the two lists of outcomes which were described in the consultation version of the regulations into one list which would capture all groups. We checked this approach with our stakeholder working group, which included members from the Care and Support Alliance and ADASS. The group concluded that it could not identify any groups that would be unintentionally excluded from eligibility due to this approach.

I turn next to the issue of informing the public, so that they have a clear understanding of their rights and the system overall. The noble Baroness will remember that we discussed this extensively during the passage of what is now the Care Act. We are putting in place a full communications campaign to ensure that people receiving services, their carers and families—and the broader population—understand the impact of the Care Act and what it means for them. The campaign will feature a partnership between the local and the national, building on the successful approaches pioneered by previous campaigns such as Change4Life. Local authorities, working with other local partners including the NHS and the voluntary sector, will get messages out directly to their own populations. We have developed a range of campaign materials and guidance to help councils communicate the changes in their local area. That will be supported by wider-reaching national activity—

Lord Geddes Portrait The Deputy Chairman of Committees
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With great respect to the noble Earl, I am afraid that a Division has been called in the Chamber. The Grand Committee stands adjourned until 4.35 pm.

16:25
Sitting suspended for a Division in the House.
16:44
Lord Geddes Portrait The Deputy Chairman of Committees
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My Lords, it is 4.35 pm. I happen to know that the Minister is on his way because I was with him in the corridor. If we could perhaps crave indulgence for just one more minute, I am sure he will appear.

16:35
Lord Geddes Portrait The Deputy Chairman of Committees
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The Minister has now rejoined us. I cut him off in mid-flow, so perhaps he would like to continue.

Earl Howe Portrait Earl Howe
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My Lords, I have only a few more remarks to make. I was explaining the measures that we would take centrally and nationally to inform the public, including door drops to 2.5 million households and articles in the national media, as well as local radio and digital activity. The first phase, which focuses on people already receiving services, began late last year and is planned to continue through to April 2016. Scoping is also under way for a behaviour change campaign to encourage people to prepare for care and support needs as part of their wider financial planning.

The noble Lord, Lord Lipsey, questioned whether the final version of the regulations described the current level of access to care and support in an adequate way. We have commissioned the PSSRU to evaluate the final version of the eligibility regulations so that we can further our understanding of their impact. It will carry out its evaluation during the summer, when the regulations have been in use for six to eight weeks, and will report in August. However, there is no reason why people currently receiving care and support have to lose their access to this because of the introduction of the national eligibility threshold. The Care Act provides people with the assurance that local authorities must meet needs that meet the national threshold and, as I mentioned earlier, authorities can also decide to meet needs that are not eligible—in other words, they can meet needs that are considered moderate. Therefore, there is flexibility for local authorities in that sense.

To the extent that I have not been able to answer questions, I shall of course write to noble Lords. However, I hope that with those comments the Committee will be sufficiently reassured to approve these sets of regulations.

Motion agreed.